Nod2-Dependent Regulation of Innate and Adaptive Immunity in the Intestinal Tract
Howard Hughes Medical Institute · University of Michigan · +2 more institutions
Abstract
The gene encoding the Nod2 protein is frequently mutated in Crohn's disease (CD) patients, although the physiological function of Nod2 in the intestine remains elusive. Here we show that protective immunity mediated by Nod2 recognition of bacterial muramyl dipeptide is abolished in Nod2-deficient mice. These animals are susceptible to bacterial infection via the oral route but not through intravenous or peritoneal delivery. Nod2 is required for the expression of a subgroup of intestinal anti-microbial peptides, known as cryptdins. The Nod2 protein is thus a critical regulator of bacterial immunity within the intestine, providing a possible mechanism for Nod2 mutations in CD.
Citation impact
- FWCI
- 51.88
- Percentile
- 100%
- References
- 35
Authors
7- KSKoichi S. KobayashiCorresponding
Howard Hughes Medical Institute, University of Michigan, Yale University, Michigan Center for Translational Pathology
- MCMathias Chamaillard
Howard Hughes Medical Institute, University of Michigan, Yale University, Michigan Center for Translational Pathology
- YOYasunori Ogura
Howard Hughes Medical Institute, University of Michigan, Yale University, Michigan Center for Translational Pathology
- OHOctavian Henegariu
Howard Hughes Medical Institute, University of Michigan, Yale University, Michigan Center for Translational Pathology
- NINaohiro Inohara
Howard Hughes Medical Institute, University of Michigan, Yale University, Michigan Center for Translational Pathology
Topics & keywords
- NOD2
- Muramyl dipeptide
- Immunity
- Innate immune system
- Regulator
- Biology
- Acquired immune system
- Gene
- Good health and well-being